Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_assertion description "[Recently, another causative gene, CISD2, has been identified in patients with a type of Wolfram syndrome (WS2) resulting in early optic atrophy, diabetes mellitus, deafness, decreased lifespan, but not diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_assertion evidence source_evidence_literature NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_assertion SIO_000772 22790102 NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_assertion wasDerivedFrom befree-20150227 NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_assertion wasGeneratedBy ECO_0000203 NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1002315.RAZ992H51wdNVK-msIU6YWQVoa3z0pXp0ueRLO2jM0bGE130_provenance.